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Volumn 80, Issue 4, 2004, Pages 799-800

Iron absorption in carriers of the C282Y hemochromatosis mutation

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; FERRITIN; TRANSFERRIN; TYROSINE; HFE PROTEIN, HUMAN; HLA ANTIGEN CLASS 1; IRON; MEMBRANE PROTEIN;

EID: 5144230879     PISSN: 00029165     EISSN: None     Source Type: Journal    
DOI: 10.1093/ajcn/80.4.799     Document Type: Editorial
Times cited : (15)

References (11)
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  • 2
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    • Iron absorption in idiopathic haemochromatosis before, during, and after venesection therapy
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  • 4
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    • Genetic hemochromatosis, a Celtic disease: Is it now time for population screening?
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  • 5
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  • 6
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    • Multicentric origin of hemochromatosis gene (HFE) mutations
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    • Rochette, J.1    Pointon, J.J.2    Fisher, C.A.3
  • 7
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    • Iron absorption by heterozygous carriers of the HFE C282Y mutation associated with hemochromatosis
    • Hunt JR, Zeng H. Iron absorption by heterozygous carriers of the HFE C282Y mutation associated with hemochromatosis. Am J Clin Nutr 2004;80:924-31.
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  • 8
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    • Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: A protective role against iron deficiency?
    • Datz C, Haas T, Rinner H, Sandhofer F, Patsch W, Paulweber B. Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency? Clin Chem 1998;44:2429-32.
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  • 9
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    • Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.